- Home
- Publications
- Publication Search
- Publication Details
Title
Whole-genome sequencing in health care
Authors
Keywords
-
Journal
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 21, Issue -, Pages S1-S5
Publisher
Springer Nature
Online
2013-05-16
DOI
10.1038/ejhg.2013.46
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Whole-genome sequencing and the physician
- (2012) A Thorogood et al. CLINICAL GENETICS
- The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe
- (2012) Ros Hastings et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Developing a policy for paediatric biobanks: principles for good practice
- (2012) Kristien Hens et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent
- (2012) Wybo Dondorp et al. HUMAN MUTATION
- The use of arrays to detect copy-number variations in clinical practice
- (2012) Birgit Sikkema-Raddatz et al. HUMAN MUTATION
- Genome-wide arrays: Quality criteria and platforms to be used in routine diagnostics
- (2012) Joris R. Vermeesch et al. HUMAN MUTATION
- Diagnostic interpretation of array data using public databases and internet sources
- (2012) Nicole de Leeuw et al. HUMAN MUTATION
- The Ethical Hazards and Programmatic Challenges of Genomic Newborn Screening
- (2012) Aaron J. Goldenberg et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- De novo mutations in human genetic disease
- (2012) Joris A. Veltman et al. NATURE REVIEWS GENETICS
- Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing
- (2012) Marco Gerlinger et al. NEW ENGLAND JOURNAL OF MEDICINE
- Incidental Medical Information in Whole-Exome Sequencing
- (2012) B. D. Solomon et al. PEDIATRICS
- Between hype and hope: whole-genome sequencing in clinical medicine
- (2012) Iris Schrijver et al. Personalized Medicine
- Noninvasive Whole-Genome Sequencing of a Human Fetus
- (2012) J. O. Kitzman et al. Science Translational Medicine
- The Predictive Capacity of Personal Genome Sequencing
- (2012) N. J. Roberts et al. Science Translational Medicine
- Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units
- (2012) C. J. Saunders et al. Science Translational Medicine
- Genetic testing and common disorders in a public health framework
- (2011) Carla G van El et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time
- (2011) Jonathan S Berg et al. GENETICS IN MEDICINE
- Preconceptional genetic carrier testing and the commercial offer directly-to-consumers
- (2011) P. Borry et al. HUMAN REPRODUCTION
- Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing
- (2011) C. J. Bell et al. Science Translational Medicine
- Communication of biobanks' research results: What do (potential) participants want?
- (2010) Tineke M. Meulenkamp et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes
- (2010) EUROPEAN JOURNAL OF HUMAN GENETICS
- Clinical assessment incorporating a personal genome
- (2010) Euan A Ashley et al. LANCET
- A map of human genome variation from population-scale sequencing
- (2010) Richard M. Durbin et al. NATURE
- A de novo paradigm for mental retardation
- (2010) Lisenka E L M Vissers et al. NATURE GENETICS
- Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy
- (2010) James R. Lupski et al. NEW ENGLAND JOURNAL OF MEDICINE
- Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing
- (2010) J. C. Roach et al. SCIENCE
- Disclosure of individual genetic data to research participants: the debate reconsidered
- (2010) Annelien L. Bredenoord et al. TRENDS IN GENETICS
- Non-invasive prenatal testing: ethical issues explored
- (2009) Antina de Jong et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Genetic testing in asymptomatic minors: recommendations of the European Society of Human Genetics
- (2009) EUROPEAN JOURNAL OF HUMAN GENETICS
- Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testing
- (2009) T Schwarzbraun et al. JOURNAL OF MEDICAL GENETICS
- Exome sequencing identifies the cause of a mendelian disorder
- (2009) Sarah B Ng et al. NATURE GENETICS
- The complete genome of an individual by massively parallel DNA sequencing
- (2008) David A. Wheeler et al. NATURE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now